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SLC17A5 Mutation
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Infantile sialic acid storage disease: Two unrelated inuit cases homozygous for a common novel SLC17A5 mutation
by
Lines, Matthew A.
,
Rupar, C. Anthony
,
Rip, Jack W.
,
Baskin, Berivan
,
Ray, Peter N.
,
Hegele, Robert A.
,
Grynspan, David
,
Michaud, Jean
,
Geraghty, Michael T.
Published 2014
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Article in Journal/Newspaper
1
Author
Baskin, Berivan
1
Geraghty, Michael T.
1
Grynspan, David
1
Hegele, Robert A.
1
Lines, Matthew A.
1
Michaud, Jean
1
Ray, Peter N.
1
Rip, Jack W.
1
Rupar, C. Anthony
1
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Topic
Fetal hydrops
1
Lysosomal storage disease
1
Neuraminidase activity
1
SLC17A5 Mutation
Sialic acid
1
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Content Provider
The University of Western Ontario: Scholarship@Western
1
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Arctic
1
Salla
1
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unknown
1
Open Polar Keyword
Arctic
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inuit
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